Psoriasis genetic testing
We are testing a new system for linking publications to authors. You can psoriasis genetic testing If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
TÁMOP-4.2.2.A-11/1/KONV-2012-0031
If you identify any major omissions or other inaccuracies in the publication list, please let us know.
Comparison of the antiremodeling effects of losartan and mirabegron in a rat model of uremic cardiomyopathy.

Scientific Reports. Genetic Investigation of Inverse Psoriasis.

Life Basel, Switzerland. Farkas K, et al. Milestones in thromboangiitis obliterans.

Frontiers in Endocrinology. Cilostazol improves the quality of life and lower-limb functional capacity also in diabetic patients Orvosi Hetilap.
Clinical trials
Thrombosis and Haemostasis. Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome. Experimental Dermatology.
Regional variation of lower limb major amputations on different geographic scales - a Hungarian nationwide study over 13 years. Zeitschrift Fur Gefasskrankheiten. The potentials and importance of imaging in large-vessel vasculitis Orvosi Hetilap. Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature. European Journal of Medical Genetics.

A Nationwide Study The management and genetic background of pityriasis rubra pilaris: a single-center experience. Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report.
Bmc Pediatrics. Nanomaterials Basel, Switzerland.

Clinical and genetic differences between pustular psoriasis subtypes. The Journal of Allergy and Clinical Immunology.
Frontiers in Immunology. Orvosi Hetilap. Effects of metabolic syndrome on arterial function in different age groups: the Advanced Approach to Arterial Stiffness study.
Tiszta test a pszoriatikus Moszkva
Journal of Hypertension. Delineating the genetic heterogeneity of OCA in Hungarian patients. European Journal of Medical Research. High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis.
Brain and Behavior. Bmc Medical Genetics. Epidemiology, difficulties of diagnosis, options for prevention and revascularization].